Unraveling the Raman Enhancement Mechanism on 1T'-Phase ReS Nanosheets.

2D transition metal dichalcogenides materials are explored as potential surface-enhanced Raman spectroscopy substrates. Herein, a systematic study of the Raman enhancement mechanism on distorted 1T (1T') rhenium disulfide (ReS ) nanosheets is demonstrated. Combined Raman and photoluminescence studies with the introduction of an Al O dielectric layer unambiguously reveal that Raman enhancement on ReS materials is from a charge transfer process rather than from an energy transfer process, and Raman enhancement is inversely proportional while the photoluminescence quenching effect is proportional to the layer number (thickness) of ReS nanosheets. On monolayer ReS film, a strong resonance-enhanced Raman scattering effect dependent on the laser excitation energy is detected, and a detection limit as low as 10 m can be reached from the studied dye molecules such as rhodamine 6G and methylene blue. Such a high enhancement factor achieved through enhanced charge interaction between target molecule and substrate suggests that with careful consideration of the layer-number-dependent feature and excitation-energy-related resonance effect, ReS is a promising Raman enhancement platform for sensing applications.